Browsing by Author "Symonds, Robert T."

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    Combined calcium looping and chemical looping combustion for post‐combustion carbon dioxide capture: process simulation and sensitivity analysis
    (Wiley, 2016-05-24) Duhoux, Benoit; Mehrani, Poupak; Lu, Dennis Y.; Symonds, Robert T.; Anthony, Edward J.; Macchi, Arturo
    In this work, a combined calcium looping and chemical looping combustion (CaL--CLC) technology is simulated at thermodynamic equilibrium conditions and the results in terms of efficiency, power production, and solids circulation rates are compared with the case of using CaL alone. In addition, a new solids looping configuration in the CaL--CLC process is proposed with the purpose of mitigating the loss of calcium oxide conversion after high cycle numbers. Simulations show an improved process efficiency of the CaL--CLC method compared with CaL alone (34.2 vs. 31.2 % higher heat value) and an increased power output (136 vs. 110 MWe additional power) due to the higher energy requirement to preheat the reactants. A sensitivity analysis of the process operating parameters highlights the particular importance of the temperature difference between reactors, which has a strong impact on the required mass of solids circulating in the loops. Finally, partial carbon dioxide capture scenarios are considered and indicate that lower capture levels are suitable to match regulation targets.
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    The effect of HCl and steam on cyclic CO2 capture performance in calcium looping systems
    (Elsevier, 2017-08-14) Symonds, Robert T.; Lu, Dennis Y.; Macchi, Arturo; Hughes, Robin W.; Anthony, Edward J.
    Calcium looping is CO2 capture technology that is considered to be technically feasible at an industrial scale using a variety of fuels such as natural gas, coals, biomass, refuse derived fuels, and biofuels. Unfortunately, many of these fuels contain significant quantities of chlorine which principally converts to gaseous HCl during combustion or gasification. To date, very few studies have examined the effect of HCl on sorbent CO2 capture performance using calcium-based sorbents under realistic carbonation and calcination conditions. In this work, experiments were conducted using thermogravimetric analysis and fixed bed reactor testing to determine the effect of HCl addition during carbonation and calcination over repeated cycles using a Canadian limestone. The presence of HCl was found to increase sorbent reactivity towards CO2 capture when steam was injected during calcination. The resulting decomposition of CaCl2 to CaO during calcination caused changes in the particle morphology, which in turn decreased the CO2 diffusional resistance during carbonation. Fixed bed test results provided confirmation of full sorbent dechlorination under typical oxy-fuel calcination conditions. It was shown that both particle surface area and pore volume were higher during tests where HCl was present during carbonation and that greater than 99% HCl capture could be achieved without adversely affecting sorbent CO2 capture performance when steam was present during both carbonation and calcination.
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    Simulation of a calcium looping CO2 capture process for pressurized fluidized bed combustion
    (Wiley, 2019-06-05) Duhoux, Benoit; Symonds, Robert T.; Hughes, Robin; Mehrani, Poupak; Anthony, Edward J.; Macchi, Arturo
    The Canadian regulations on carbon dioxide emissions from power plants aim to lower the emissions from coal‐fired units down to those of natural gas combined cycle (NGCC) units. Since coal is significantly more carbon intensive than natural gas, coal‐fired plants must operate at higher net efficiencies and implement carbon capture to meet the new regulations. Calcium looping (CaL) is a promising post‐combustion carbon capture (PCC) technology that, unlike other capture processes, generates additional power. By capturing carbon dioxide at elevated temperatures, the energy penalty that carbon capture technologies inherently impose on power plant efficiencies is significantly reduced. In this work, the CO2 capture performance of a calcium‐based sorbent is determined via thermogravimetric analysis under relatively high carbonation and low calcination temperatures. The results are used in an aspenONE™ simulation of a CaL process applied to a pressurized fluidized bed combustion (PFBC) system at thermodynamic equilibrium. The combustion of both natural gas and coal are considered for sorbent calcination in the CaL process. A sensitivity analysis on several process parameters, including sorbent feed rate and carbonator operating pressure, is undertaken. The energy penalty associated with the capture process ranges from 6.8 –11.8 percentage points depending on fuel selection and operating conditions. The use of natural gas results in lower energy penalties and solids circulation rates, while operating the carbonator at 202 kPa(a) results in the lowest penalties and drops the solids circulations rates to below 1000 kg/s.